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Development of Coronary Pulse Wave Velocity: New Pathophysiological Insight Into Coronary Artery Disease

BACKGROUND: Although aortic stiffness assessed by pulse wave velocity (PWV) is a strong predictor of coronary artery disease, the significance of local coronary stiffness has never been tackled. The first objective of this study was to describe a method of measuring coronary PWV (CoPWV) invasively a...

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Autores principales: Harbaoui, Brahim, Courand, Pierre‐Yves, Cividjian, Andrei, Lantelme, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5523779/
https://www.ncbi.nlm.nih.gov/pubmed/28154161
http://dx.doi.org/10.1161/JAHA.116.004981
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author Harbaoui, Brahim
Courand, Pierre‐Yves
Cividjian, Andrei
Lantelme, Pierre
author_facet Harbaoui, Brahim
Courand, Pierre‐Yves
Cividjian, Andrei
Lantelme, Pierre
author_sort Harbaoui, Brahim
collection PubMed
description BACKGROUND: Although aortic stiffness assessed by pulse wave velocity (PWV) is a strong predictor of coronary artery disease, the significance of local coronary stiffness has never been tackled. The first objective of this study was to describe a method of measuring coronary PWV (CoPWV) invasively and to describe its determinants. The second objective was to assess both CoPWV and aortic PWV in patients presenting with acute coronary syndromes or stable coronary artery disease. METHODS AND RESULTS: In 53 patients, CoPWV was measured from the delay in pressure wave and distance traveled as a pressure wire was withdrawn from the distal to the proximal coronary segment. Similarly, aortic PWV was measured invasively when the wire was pulled across the ascending aorta; carotid–femoral PWV was also measured noninvasively using the SphygmoCor system (AtCor Medical). Mean CoPWV was 10.3±6.1 m/s. Determinants of increased CoPWV were fractional flow reserve, diastolic blood pressure, and previous stent implantation in the recorded artery. CoPWV was lower in patients with acute coronary syndromes versus stable coronary artery disease (7.6±3 versus 11.5±6.4 m/s; P=0.02), and this persisted after adjustment for confounders. In contrast, aortic stiffness, assessed by aortic and carotid–femoral PWV, did not differ significantly. CONCLUSIONS: CoPWV seems associated with acute coronary events more closely than aortic PWV. High coronary compliance, whether per se or because it leads to a distal shift in compliance mismatch, may expose vulnerable plaques to high cyclic stretch. CoPWV is a new tool to assess local compliance at the coronary level; it paves the way for a new field of research.
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spelling pubmed-55237792017-08-14 Development of Coronary Pulse Wave Velocity: New Pathophysiological Insight Into Coronary Artery Disease Harbaoui, Brahim Courand, Pierre‐Yves Cividjian, Andrei Lantelme, Pierre J Am Heart Assoc Original Research BACKGROUND: Although aortic stiffness assessed by pulse wave velocity (PWV) is a strong predictor of coronary artery disease, the significance of local coronary stiffness has never been tackled. The first objective of this study was to describe a method of measuring coronary PWV (CoPWV) invasively and to describe its determinants. The second objective was to assess both CoPWV and aortic PWV in patients presenting with acute coronary syndromes or stable coronary artery disease. METHODS AND RESULTS: In 53 patients, CoPWV was measured from the delay in pressure wave and distance traveled as a pressure wire was withdrawn from the distal to the proximal coronary segment. Similarly, aortic PWV was measured invasively when the wire was pulled across the ascending aorta; carotid–femoral PWV was also measured noninvasively using the SphygmoCor system (AtCor Medical). Mean CoPWV was 10.3±6.1 m/s. Determinants of increased CoPWV were fractional flow reserve, diastolic blood pressure, and previous stent implantation in the recorded artery. CoPWV was lower in patients with acute coronary syndromes versus stable coronary artery disease (7.6±3 versus 11.5±6.4 m/s; P=0.02), and this persisted after adjustment for confounders. In contrast, aortic stiffness, assessed by aortic and carotid–femoral PWV, did not differ significantly. CONCLUSIONS: CoPWV seems associated with acute coronary events more closely than aortic PWV. High coronary compliance, whether per se or because it leads to a distal shift in compliance mismatch, may expose vulnerable plaques to high cyclic stretch. CoPWV is a new tool to assess local compliance at the coronary level; it paves the way for a new field of research. John Wiley and Sons Inc. 2017-02-02 /pmc/articles/PMC5523779/ /pubmed/28154161 http://dx.doi.org/10.1161/JAHA.116.004981 Text en © 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Harbaoui, Brahim
Courand, Pierre‐Yves
Cividjian, Andrei
Lantelme, Pierre
Development of Coronary Pulse Wave Velocity: New Pathophysiological Insight Into Coronary Artery Disease
title Development of Coronary Pulse Wave Velocity: New Pathophysiological Insight Into Coronary Artery Disease
title_full Development of Coronary Pulse Wave Velocity: New Pathophysiological Insight Into Coronary Artery Disease
title_fullStr Development of Coronary Pulse Wave Velocity: New Pathophysiological Insight Into Coronary Artery Disease
title_full_unstemmed Development of Coronary Pulse Wave Velocity: New Pathophysiological Insight Into Coronary Artery Disease
title_short Development of Coronary Pulse Wave Velocity: New Pathophysiological Insight Into Coronary Artery Disease
title_sort development of coronary pulse wave velocity: new pathophysiological insight into coronary artery disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5523779/
https://www.ncbi.nlm.nih.gov/pubmed/28154161
http://dx.doi.org/10.1161/JAHA.116.004981
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